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Cannabinoids: A New Group of Agonists of PPARs

Cannabinoids have been used medicinally and recreationally for thousands of years and their effects were proposed to occur mainly via activation of the G-protein-coupled receptor [Formula: see text] (cannabinoid receptor 1/2). Discovery of potent synthetic analogs of the natural cannabinoids as clin...

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Detalles Bibliográficos
Autores principales: Sun, Yan, Bennett, Andy
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2220031/
https://www.ncbi.nlm.nih.gov/pubmed/18288264
http://dx.doi.org/10.1155/2007/23513
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author Sun, Yan
Bennett, Andy
author_facet Sun, Yan
Bennett, Andy
author_sort Sun, Yan
collection PubMed
description Cannabinoids have been used medicinally and recreationally for thousands of years and their effects were proposed to occur mainly via activation of the G-protein-coupled receptor [Formula: see text] (cannabinoid receptor 1/2). Discovery of potent synthetic analogs of the natural cannabinoids as clinically useful drugs is the sustained aim of cannabinoid research. This demands that these new compounds be free of the psychotropic effects that connected with the recreational use of cannabinoids. In preclinical studies cannabinoids displayed many of the characteristics of nonsteroidal anti-inflammatory drugs (NSAIDs) and it seems to be free of unwanted side effects. An increasing number of therapeutic actions of cannabinoid are being reported that do not appear to be mediated by either [Formula: see text] or [Formula: see text] , and recently nuclear receptor superfamily PPARs (peroxisome-proliferator-activated receptors) have been suggested as the target of certain cannabinoids. This review summarizes the evidence for cannabinoid activation on PPARs and possible associated remedial potentials.
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spelling pubmed-22200312008-02-20 Cannabinoids: A New Group of Agonists of PPARs Sun, Yan Bennett, Andy PPAR Res Review Article Cannabinoids have been used medicinally and recreationally for thousands of years and their effects were proposed to occur mainly via activation of the G-protein-coupled receptor [Formula: see text] (cannabinoid receptor 1/2). Discovery of potent synthetic analogs of the natural cannabinoids as clinically useful drugs is the sustained aim of cannabinoid research. This demands that these new compounds be free of the psychotropic effects that connected with the recreational use of cannabinoids. In preclinical studies cannabinoids displayed many of the characteristics of nonsteroidal anti-inflammatory drugs (NSAIDs) and it seems to be free of unwanted side effects. An increasing number of therapeutic actions of cannabinoid are being reported that do not appear to be mediated by either [Formula: see text] or [Formula: see text] , and recently nuclear receptor superfamily PPARs (peroxisome-proliferator-activated receptors) have been suggested as the target of certain cannabinoids. This review summarizes the evidence for cannabinoid activation on PPARs and possible associated remedial potentials. Hindawi Publishing Corporation 2007 2007-11-15 /pmc/articles/PMC2220031/ /pubmed/18288264 http://dx.doi.org/10.1155/2007/23513 Text en Copyright © 2007 Y. Sun and A. Bennett. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sun, Yan
Bennett, Andy
Cannabinoids: A New Group of Agonists of PPARs
title Cannabinoids: A New Group of Agonists of PPARs
title_full Cannabinoids: A New Group of Agonists of PPARs
title_fullStr Cannabinoids: A New Group of Agonists of PPARs
title_full_unstemmed Cannabinoids: A New Group of Agonists of PPARs
title_short Cannabinoids: A New Group of Agonists of PPARs
title_sort cannabinoids: a new group of agonists of ppars
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2220031/
https://www.ncbi.nlm.nih.gov/pubmed/18288264
http://dx.doi.org/10.1155/2007/23513
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